Supplementing Hearing Aids With Computerized Auditory Training

Not Applicable

Completed

Conditions: Hearing Loss

Interventions: Behavioral: CONTROL
Behavioral: Lace-DVD
Behavioral: PLACEBO-Directed listening
Behavioral: LACE-computer

Registration Number: NCT00727337

Lead Sponsor: VA Office of Research and Development

Brief Summary: The study is designed to examine the effectiveness of a computer-based auditory training program to improve the benefits received by individuals who wear hearing aids. The study will involve 3 groups - a computer-based training group, an active listening group which will involve listening to books on CD, and a placebo group that receives no additional treatment.

Detailed Description: This proposed study is a multi-site, single-masked (blinded), randomized controlled, parallel group clinical trial to assess the effectiveness of an at home PC-based auditory training as a supplement to standard-of-care hearing-aid intervention in veterans treated for hearing loss, with or without previous hearing-aid experience. The participants will be assigned randomly to one of three groups, with hearing-aid use stratified within the groups: (1) Group 1, HA+AT, in which the participants will receive standard-of-care hearing-aid intervention (HA) and complete the four-week LACE auditory training program (AT); (2) Group 2, HA, with the participants receiving only standard-of-care hearing-aid intervention (HA); and (3) Group 3, HA+DL, in which the participants will receive standard-of-care hearing-aid intervention (HA) and complete four-weeks of placebo auditory training, consisting of directed listening (DL) to books-on-tape. The participants in each group will attend four test sessions. During Session 1 the informed consent process will be completed, baseline assessments will be made to ensure that the participants meet the study inclusion criteria (page 52), testing of predictor variables (page 57-58) will be completed, and all hearing aids will be assessed for correct functionality (page 53). The participants then will be assigned randomly to a study group. Session 2 will occur four weeks after Session 1. During Session 2, baseline performance on the outcome measures will be assessed (page 54-57), as will performance on the predictor variables. Following testing, the participants in Groups 1 and 3 will receive training in the use of the AT or DL programs. Session 3 will occur at the end of the 4-week experimental training period. During Session 3 all participants will be retested on the outcome measures to assess short-term intervention outcomes. During Session 4, which will occur at seven-months post-study enrollment (i.e., six-months post training completion for Groups 1 and 3), all participants will be retested on all outcome measures to examine the long-term outcomes. In Sessions 2-4, the stability of hearing-aid function will be assessed through electroacoustic measures.

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 279

Inclusion Criteria

adult onset hearing loss,
English as the first language,
bilateral, symmetric, sensorineural hearing loss,
average audiometric thresholds for 500, 1000, and 2000 Hz less than 50-dB HL in either ear,
aided speech recognition in quiet of 40% binaurally,
appropriate cognitive skills assessed using the Mini Mental State Exam (Folstein et al., 1975) with age/education norms (Crum et al., 1993),
adequate vision to participate in the study as determined with the Smith-Kettlewell Institute Low Luminance (SKILL) Card,
eligible for VA-issued hearing aids.

Exclusion Criteria

known neurological, psychiatric disorders, or co-morbid diseases that would prevent completion of the study as determined by chart review,

Study & Design

Study Type: INTERVENTIONAL

Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
CONTROL	CONTROL	Participants will be provided with hearing aids
LACE-DVD	Lace-DVD	Participants will complete the LACE training, however, not in an interactive computer mode but through a static DVD mode
PLACEBO-DIRECTED LISTENING	PLACEBO-Directed listening	Participants will complete a directed listening to books on CD treatment
LACE-COMPUTER	LACE-computer	Participants will complete a computer-based auditory training program (i.e., LACE)

Primary Outcome Measures

Name	Time	Method
Words-in-Noise Test (WIN) Change	Baseline, immediate post-intervention (up to 2 to 6 weeks), 6 month follow up	Monosyllabic words (NU-6 female version) with a carrier phrase were presented auditory only in a multitalker babble.The participant is asked to repeat the last word of each phrase. The total number of correct words is input into the Spearman-Karber equation to derive a 50% point. This is the signal-to-noise ratio in dB that an individual requires to get 50% of the words correct. This test was completed at baseline and follow up visits.

Secondary Outcome Measures

Name	Time	Method
Hearing Handicap Inventory for the Elderly (HHI) Change	Baseline, immediate post-intervention (up to 2 to 6 weeks), 6 month follow up	The HHI is a 25-item questionnaire that assesses the social and emotional consequences of hearing loss. The HHI for the elderly is for individuals age 65 years and older (Ventry \& Weinstein 1982); the HHI for adults is for individuals aged 64 years and younger (Newman et al. 1990). The versions differ in the wording of three questions. The participants were asked to complete the appropriate HHI for aided listening to reflect their residual hearing handicap. HHI items are answered on a scale of Yes (4 points), Sometimes (2 points) and No (0 points), with higher scores indicating greater reported hearing handicap. Total HHI scores, which can range from 0 to 100, were used for all analyses.
Abbreviated Profile of Hearing Aid Benefit (APHAB) Change	Baseline, immediate post-intervention (up to 2 to 6 weeks), 6 month follow up	The Abbreviated Profile of Hearing Aid Performance (APHAP; Cox \& Alexander 1995) was used to assess activity limitations and the Hearing Handicap Inventory for the Elderly or Adults (HHI; Ventry \& Weinstein 1982; Newman et al. 1990) was used to assess participation restrictions. The APHAP is a 24-item questionnaire that documents hearing difficulties in specified listening situations. The items are answered on a 7-point scale from 'Always' (or 99%) to 'Never' (or 1%) with higher scores indicating greater reported hearing difficulty. The APHAP global score that ranges from 1 to 99 was used for all analyses.